# Genetikum

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/genetikum/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 66 |
| Citations | 65,410 |
| City | Neu-Ulm |
| Country | DE |
| Description | Genetikum is a research organisation in Neu-Ulm, DE. OpenAlex records 1,522 works and 65,410 citations for it. 285 researchers list it as their most recent affiliation. |
| Homepage | https://genetikum.de |
| OpenAlex ID | https://openalex.org/I4210104571 |
| Region | Bavaria |
| Researchers | 285 |
| ROR ID | https://ror.org/015thzh02 |
| Type | facility |
| Works | 1,522 |

## University papers

- [Polycystic kidney disease](https://scholariq.org/papers/polycystic-kidney-disease-2/)
- [PKHD1, the Polycystic Kidney and Hepatic Disease 1 Gene, Encodes a Novel Large Protein Containing Multiple Immunoglobulin-Like Plexin-Transcription–Factor Domains and Parallel Beta-Helix 1 Repeats](https://scholariq.org/papers/pkhd1-the-polycystic-kidney-and-hepatic-disease-1-gene-encodes-a-novel-large/)
- [Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome](https://scholariq.org/papers/clinical-and-molecular-phenotype-of-aicardi-goutieres-syndrome/)
- [TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum](https://scholariq.org/papers/ttc21b-contributes-both-causal-and-modifying-alleles-across-the-ciliopathy/)
- [Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta](https://scholariq.org/papers/exome-sequencing-identifies-truncating-mutations-in-human-serpinf1-in-autosomal/)
- [Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening](https://scholariq.org/papers/non-invasive-prenatal-testing-for-aneuploidy-and-beyond-challenges-of/)
- [Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)](https://scholariq.org/papers/clinical-consequences-of-pkhd1-mutations-in-164-patients-with-autosomal/)
- [Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia](https://scholariq.org/papers/loss-of-nephrocystin-3-function-can-cause-embryonic-lethality-meckel-gruber-like/)
- [Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy](https://scholariq.org/papers/candidate-exome-capture-identifies-mutation-of-sdccag8-as-the-cause-of-a-retinal/)
- [A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies](https://scholariq.org/papers/a-common-allele-in-rpgrip1l-is-a-modifier-of-retinal-degeneration-in/)
- [Lifelong effect of therapy in young patients with the <i>COL4A5</i> Alport missense variant p.(Gly624Asp): a prospective cohort study](https://scholariq.org/papers/lifelong-effect-of-therapy-in-young-patients-with-the-i-col4a5-i-alport-missense/)
- [Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases Cohort](https://scholariq.org/papers/description-and-cross-sectional-analyses-of-25-880-adults-and-children-in-the-uk/)

## University researchers

- [Carsten Bergmann](https://scholariq.org/researchers/carsten-bergmann/)

## University top topics

Showing 8 of 25.

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Prenatal Screening and Diagnostics](https://scholariq.org/topics/prenatal-screening-and-diagnostics/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [RNA and protein synthesis mechanisms](https://scholariq.org/topics/rna-and-protein-synthesis-mechanisms/)
- [DNA Repair Mechanisms](https://scholariq.org/topics/dna-repair-mechanisms/)
- [Fungal and yeast genetics research](https://scholariq.org/topics/fungal-and-yeast-genetics-research/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [RNA Research and Splicing](https://scholariq.org/topics/rna-research-and-splicing/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.